BRUNS RING CURETTE 1271-147

GUDID 00192896092129

BRUNS RING CURETTE

SONTEC INSTRUMENTS, INC.

Bone curette, reusable

• Primary Device ID: 00192896092129
• NIH Device Record Key: 4c9322db-3098-42f6-a19a-715488e8f98f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BRUNS RING CURETTE
• Version Model Number: 1271-147
• Catalog Number: 1271-147
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 9 Inch
• Length: 9 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896092129 [Primary]

FDA Product Code

• HTF: CURETTE

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00192896092129]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-10-04
• Device Publish Date: 2018-11-22

On-Brand Devices [BRUNS RING CURETTE]

• 00192896092129: BRUNS RING CURETTE
• 00192896092112: BRUNS RING CURETTE
• 00192896092105: BRUNS RING CURETTE